I am 26 yrs old and contracted HBV vertically. I am new to this site, but am due to start the pegylated interferon alfa-2a treatment (Pegasys) this Friday and am terrified of the side effects. This treatment is usually used to treat HCV, but I have chosen it over the antiviral pills b/c of the lack of risk of viral tolerance and the dangers connected to skipping doses or quitting an antiviral pill treatment.
As I have read the forums related to HBV, I have not seen any posts regarding others who have chosen to go on this Pegasys treatment as I have. I was wondering if any of you could please respond to my post in regards of whether or not you were ever offered Pegasys (interferon), and if you were offered, how you decided on the treatment option that you did.
I am a 3rd year full-time student doing a double major in Biology and Radiation Therapy. Can anyone out there provide me with your personal experiences on Pegasys and whether or not you were able to continue with a busy schedule? Am I being too optimistic to continue with even a 15 credit hr load?
the choice is good and if you cannot stand sides you can stop it, what is your hbv state and your hbsag titter?
my sister and my mother tried interferon 10-20 years ago and sides were very very heavy (especially mental disorders), but i also met young people with no sides at all. you have more chances to lose hbsag with this txso if you can go for it
i started with entecavir because i cannot stand interferon for my job and don't know the level of fibrosis if f2 or f4 because i had a very alt flare, i count to switch on combo as trial results from entecavir-tenofovir sides are available (results oct 2010/end of trial 2012)
Hello Ambiance. I've been reading this forum,because my husband has a chronic HBV. He's 46 now and has started Viread about 4-5 months ago. He was not offered Interferon, but he wouldn't accepted it, anyways. It's just him. He rather takes a pill once a day,without the side effects,than goes on Interferon therapy for 11 months. That's just his personal choice. But you're a young person and I don't think going on antivirals for, most likely, the rest of your life would be a good decision. But I'm not a doctor and don't now your VL or ALT,AST,HbeAg status and other results. Have you had a genotyping done? I have read somewhere that genotyping might have an effect on Interferon treatment. Genotypes A,B,C with high ALT and low viral load react well to Interferon treatment,where genotype D -doesn't.
Ambiance, 3 months ago I have finished 48 weeks of Pegylated Interferon and Ribavirin therapy for my HCV (PEG/RBV). I consider myself doing quite well on that therapy. I've encounter some "bumps" here and there but nothing major. That was just me. Everybody reacts differently and you won't now about your reaction until you start.:) If the side effects will be unbearable,you can always stop. Please educate yourself about all possible side effects and make sure your close ones are aware of it too. You might need their physical and emotional support. I hope I don't scare you,I just want you to be prepared. That's all. Wishing you good luck with the treatment and getting rid of the virus FOREVER!:)
P.s. My husband's response after 3 month of Viread treatment is: UND.:)
I took Pegasys from January to June of 2009 in 24 shots. I'm 27 years old and have had, until now, no notable sideeffects. Exceptions are two instances, one after the first shot and other week before the last shot. But I could easily carry on with my normal life.
Also, my gasterenterologist advised me that interferon is the most up-to-date and effective thing available in our country.
I just started my treatment this evening...It's been about an hour and a half and it seems that I don't have any symptoms thus far.
Thanks so much for all your responses :) I am very nervous about this, and my poor husband did a weak job of trying to talk me out of it as I was administering my first injection. I will update tomorrow. Thanks again.
I tried alfa-interferon for four months to treat hep-B, and my thyroid profile test became abnormal, so I had to discontinue the treatment. My viral load was too high, it went from 300,000,000 copies to 50,000,000 copies, at the time I stopped using it. Some people tolerate it very well, and have no side effects. The advantage to interferon is seroconversion, and there is some evidence that it reduces the risk of carcinoma, even if it doesn't clear the virus.
check my posts about vienna congress, now it is possible to know if you will benefit from interferon or not in 24weeks from hbsag/hbdna quantity
the pros of trying interferon are hbsag lower that 1500iu/ml because you have chances of hbsag seroconversion, so they just monitor hbsag and hbvdna drop in the first 12-24 weeks and if there is no responce you can stop it
the cons, high hbsag and high hbvdna load are not suppressed by interferon and sides depend on age and are different from person to person.
i will be starting it in 2-4 months, i have started with entecavir but i went to the research center who made these studies and since my hbsag is only 300iu/ml they will put me on interferon/entecavir combo or interferon mono.at the moment i am on etv+alinia combo
see all posts about interferon/alinia/tdf/etv, there are pros and cons but antivirals have almost 0% rates of seroconversion and life thrapy so i will choose them as a last chance
i think there aren't a lot of posts about interferon because of the high cost of interferon and the high income for pharma companies from life antiviral therapy, so in US the market is all for antivirals
it is the contrary in europe, the drugs are free and interferon is the first choice and if it fails antivirals are the second option
Hi there I hope it goes as well for you as did for me today. I have been on treatment for HepC for 6 months and 1 week. My doctor told me today I am as good as cured. I take treatment until July 1. Then that is it. I go back every 6 months for the next 4 years. After 5 weeks I was undectable. And I was Gentoype 1 that hardest one to treat.
I have only missed 3 days of work in all these months. I hope you do as well as I did.
Did you lower your virus load and got seroconversion? I took entacavir for almost a year and hit a plateau and now under Pegasys once a week. My husband got non detect in virus load after taking entacavir. So, he doesn';t need to be on Pegasys (interferon). I am yet to go in for the first blood test in a few days
My husband got non detect in virus load after taking entacavir
hbvdna is not the virus or infected cells, it is only replication but the virus is still infecting liver cells.entecavir is very good to stop liver damage, i am on it too, but it doesn t clear infected cells on most patients it increases infected cells
pegasys clears infected cells but not enough potent to stop liver damage in many cases
the best therapy to try clear infected cells and stop liver damage done by virus replication is a combo of etv+pegasys
I am chr hep b, male 29, i was on teraphy (pegasys and lamivudin) 48 weeks,
After 48 weeks i am HbsAg negative HbeAg negative, anti-HbsAg negative and anti-HbeAg negative.
After 52 weeks i am anti-HbsAg positive titer>1000.
Thanks for your thinking. But in my brothers case it was not good enough. He had 80 mg per week doges for 24 weeks. DNA cleared but HBSAG (Australia Antigen) increases to double 100000 iu. We all wishes for high achievement but left heartbroken. He is now on going Entecavir to reduced ALT. Wish him good luck.
is it true that one has hairloss by interferon? my doc is going to start interferon from next week ...worried...my dna count is zero but recently i converted from hbeag negative to positive which he says is pretty impossible so decided to switch me from entecavir to interferon :-(
some have but it is just the hair getting thinner, it is not exactly hair loss and
all the hair comes back
but recently i converted from hbeag negative to positive.....
maybe you converted hbeag negative, if you converted hbeag positive you have wildtype virus and not mutans.
anyway hbeag pos or neg doesn t make much difference, pos is better
which he says is pretty impossible so decided to switch me from entecavir to interferon :-(
how stupid doctor combo is the only way to clear hbv, entecavir mono will never clear hbv (only 5%) and intf mono pretty much the same (7-10%) while combo can reach 50% of hbv clearance.if doctors says these are on study now ombo trials date back since 2004 and earlier
actually when i was detected hbsag positive four yrs back i was found to be hbeag negative with high hbv dna count , so he started with adefovir n it worked well for a yr but after that dna levels started to increase again so he switched me to entecavir , it worked well my dna viral load constantly was zero for three yrs with hbeag negative and anti hbeag positive ... but recently n november when he was planning to stop the treatment my hbeag turned to be positive which he says is impossible when dna viral load is zero so decided to to go for interferon :-(
Thanks for the information. Reversion of HbeAg is not unheard of, but I can find very little information about its clinical significance. I wonder whether it is possible that the lab had made a mistake? In November, did you test your hbvdna and ALT?
As for Interferon treatment, as it is finite course of treatment, with manageable side effects in most cases, I don't see any harm in trying it. But I always want to know what the treatment hopes to achieve. If available, I would suggest getting a quantitative assay of HBsAg, and a re-test of your hbvdna, ALT, and HBeAg status before starting Interferon.
hbeag reversion is impossible with bcp and precore mutants but it is normal if you are wildtype
in the wildtype case the patient is hbeag negative because of antibodies hbeab but if immune system gets suppressed or the virus antigens get superior to the antibodies you get hbeag pos again
in my family:
one used to get hbeag pos again all the time when hbvdna detactable
i was hbeag neg and hbeab neg at 16-17yo but became hbeag pos at about 18-19 and then hbeag neg after 6 months of alt at 1500.hbv simply mutated to precore or bcp at that time
your doctor is a killer, change it right away or sue him if possible:
using adefovir he made you resistant to both adefovir and reduced response to tenofovir
using entecavir monotherapy you risk resistance to entecavir low but possible, lamivudine, telbivudine
to be safe you should be on entecavir plus tenofovir, entecavir will be active on the adefovir mutation and the possible tenofovir resistance mutations while tenofovir will protect you from entecavir, lamivudine, telbivudine resistance mutations
interferon add on to entecavir plus tenofovir or entecavir plus interferon can be good only if your hbsag is low in the 1000iu/ml range, if hbsag is 1000 to 10.000iu/ml it is not sure to work on hbsag
another important test is precore/bcp mutants test, adefovir, lamivudine and entecavir mutants test and genotype test
if you have no precore/bcp mutants your hbeag positive status will have 16% hbv clearance with the use of tenofovir plus entecavir, 24% tenofovir plus entecavir plus interferon.i consider the use of tenofovir plus entecavir because you do have adefovir resistance which reduces response to tenofovir
In one Taiwan study, 283 patients were followed for a median period of 8.6 years after HBeAg seroconversion, 4.2% had HBsAg reversion. I have a feeling that these occurred in the immediate period after seroconversion. It is hard to understand HBeAg reversion in the setting of very low hbvdna.
hbeag is produced similar to hbsag, indipendently from virions (hbvdna).this in wild type and you can have hbeag pos, hbeag neg with hbeab pos and both negative if antibodies and antigenes are in balance
remember that you can be hbvdna und but no decrease of hbeag
with the precore bcp the hbeag is reduced or not produced so any hbeab is ble to hide hbeag in blood
the easiest thing is follow hbsag quantity when it reaches values less than 1000iu/ml for genotype d the hbv virus is really inactive and it is very difficult to have both hbvdna high again or hbeag reversion
i consider the use of tenofovir plus entecavir because you do have adefovir resistance which reduces response to tenofovir
but i was on entecavir for last three yrs is it ok if i continue entecavir plus tenofovoir from this point...as i need to plan for babies too...i heard its not safe to use tabs while u r pregnant :-(...doc was saying as u plan to have babies if interferon works that would be a plus point and that if after three months we find it not working we can immediately withdraw the interferon injections and will give me tenofir which is safe during pregnancy...i am a lot confused plij suggest what shall i ask my doc to do?...:-(
it is best to take entecavir plus tenofovir and stop entecavir while you get pregnant (allow more than 6months on this combo).
my recent results were - hbeag positive ( which was negative for four yrs)
anti hbeag positive
check that hbeag becomes negative again on the combo.if both hbeag and hbeab remain positive this is another mutant, dont remember which one but it is not good for sure
hbsag 250 iu/ml
this is not hbeag quantity but the limit of abbott architect without diluition of your blood sample.the lab was so stupid and lazy to avoid the diluition and just tell you your hbsag is superior to 250iu/ml which is a totally useless information because if you have chronic hbv hbsag is in the thousands as 99,9% of hbv carriers
recheck hbsag with diluition
there is no resistance to tenofovir only reduced response on one type of mutant from adefovir but even if reduced response most get hbvdna und
interferon doesn t work if hbsag is high it makes sense to use interferon only to clear hbv as add on to long time use of tenofovir or entecavir.tenofovir plus entecavir will rescue your immune system response in a few years use so that add on of intf may work
both hbeag and hbeab positive:
probably not a mutant, it can be a balance between hbeag and hbeab and even if it is the mutant it is not dangerous at all as long as hbvdna is und and it is of course treatable
i am really thankful to you for guiding me ... :-) i am surely going to talk to my doc on all this ....sometimes i regret a lot for having this ... why me :-( i donno how i got this where on this earth from??..but least what i can do is just to move on with this rest of my life ....
when you talk to the doctor be aware that most say:
"we wait for the resistance to make combination therapy if the test shows resistance we make combo"
of course this is totally bull**it nonsense, the combo must be used in order to prevent the resistance mutations once they happen there is no way back to the wild virus, so even if resitsance can be treated by combo it is best to prevent it
i suggest this so you know what to tell to the doctor, i too had to fhight to convince them on the combo......
guess what ...my recent results --> hbvdna is 18 iu/ml...my dna was zero from last 3 yrs ..but 6months back my hbeag turned positive n now dna count is 18...does this mean virus has grown resistant to entacavir now???? :-(
anti hbe is positive ..hbsag positive(cov=0.152, od=1.740) and hbv dna 18iu/ml...asl=37 , alt=38...my doc he is insisting on interferon only ...he is saying see for months doesn't work will give you tenofir....he is saying combination medi's are still under doubt...but he has left the decition with us whether interferon or medicine ....plij one last booster advice for me :-/
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